HuagongsheHuagongshe Chemistry Print Report · For research reference only
N-(3-bromophenyl)-7-fluoropyrido[4,3-d]pyrimidin-4-amine → N-(3-bromophenyl)-7-methoxypyrido[4,3-d]pyrimidin-4-amine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | N-(3-bromophenyl)-7-fluoropyrido[4,3-d]pyrimidin-4-amine | HCID 5328251 | — |
| Reactant | Sodium methanolate methanol | HCID 23694274 | — |
| Product | N-(3-bromophenyl)-7-methoxypyrido[4,3-d]pyrimidin-4-amine | HCID 5328254 | 89% |
Reaction Steps
A solution of 7-fluoro-4-(3-bromoanilino)pyrido[4,3-d]pyrimidine (100 mg, 0.31 mmol) in 1 M sodium methoxide-methanol (30 mL) is stirred under reflux for 42 h. The resulting mixture is concentrated under reduced pressure, diluted with water and neutralized with dilute HCl to give 7-methoxy-4-(3-bromoanilino)pyrido[4,3-d]pyrimidine (92 mg, 89%) as a white solid. 1H NMR (DMSO) δ 10.22 (1H, brs), 9.57 (1H, s), 8.63 (1H, s), 8.19 (1H, s), 7.86 (1H, brd, J=7.9 Hz), 7.39 (1H, t, J=7.9 Hz), 7.35 (1H, dd, J=7.9, 1.5 Hz), 6.96 (1H, s), 4.00 (3H, s).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06521620B1 |
| Source dataset | uspto-grants-2003_02 |
| ORD ID | ord-db2e568fb2104d28bcd41025f64459b6 |
| Source note | uspto-grants-2003_02 |